Tag | Content |
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EnhancerAtlas ID | HS060-28519 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:159869720-159871300 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX20 | MA0689.1 | chr5:159870481-159870492 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr5:159870482-159870492 | TTCACACCTT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_32669 | chr5:159867373-159871572 | GM12878 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I160440 | chr5 | 159867374 | 159871572 |
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Enhancer Sequence | CAGAAACCAG TCCTGGCTGA TTTAAGCAGA AAAGGAATCA ATTGAGAGCA TGTCAAGTGG 60 TTCAGAGAAA TGCCAGGAAA ATGATAGAAG AGGCACCAGA TAAAGGGAGG TAACAAGGAA 120 GGTCAGGCAT CGGCCAGGGT AGCAGTCTGG GTGATGACAC AGCGCCAACC TGGCATGGAT 180 GCCACTGACA CTGAAAACCC TAGCTTACAC AGCCAGCACA GGTGACACAG GATGCTGCTG 240 CTATTGCTGC CACTATTACG ATGGGTTCAT GGCATATGCA TATCTAATTG GTTGAACCTG 300 GGTCATGTCC TCAACCATCC CTGACACTTT CAAATTCTAT GGTGGGAGGT GCTCTCTGCT 360 TCCCACCAAG ACTCTTAAGT GGGGGAATTC CTCCAACAAC TGAAGGCAGC CCTCCAAAGT 420 CAACTAATAG TCAGCAGGAA CAGAAACCAG CTTGAGCTAG CTTTAGTATA AAAGACTCTT 480 TCAGGCTATT GGGTGTTTCA TGAAACAAAG AACAGGAGGG AAGCCAGGCC TTTGGGAGGG 540 CGTGGAGCCA AGTACTTGAA AGTCAAAGAA CTCTTTTCCC AACTCTCACC TCTGCTTCTC 600 TGTGCTCCTT CTTCACTTCT TTCTCTCTGC ATTATGACAC TTCATTCCCT CAGTCCAGGA 660 GATGGGATCA GGTGGTCTTT GGAAAGGCTT CCTCCCATGG CTCAAAGGAC ACCTCCTAGA 720 AAAGCAAGGC AGGCATTCAC TACGGGGTGG CTTCCTGCCC CCTTCACACC TTCATTCTGG 780 TCACTCAGCT TGGGTGTCTG CTGTTTGATA CTGTTTTCTT CTCCACTCTC TGCTGAGGTC 840 CCTTTAGATA GCCTGAATAT CCCTCTTCGT ATCTCTCTGA GGCTGCAGGT GGAGGCTCAT 900 ATATTCCTAG AATGTTAGGC CTTCGTTTTA CAGATGCACA GTCTGAGGCC TAAGAAATTA 960 AGTGACTTAC TCGAGATTCT GACTGTCCCA TGAATGGGTT GGAACATGGT GCTTAGCATG 1020 TAGAAAGCTC TCAGTAGACT TTAGTTATGT CATTCAGATT TCTTTTAATT CAAAGCACAT 1080 TCCTTTCCTT TTCTCTCTTT TGTTCTCATG GCTCTCTTTC TCCACTATTT ATTTGTCCTT 1140 TCCAAAAATA TATACTGAAG GCCTTCTGTG TGCCTGGTAA TATTGTCGAT GCTGGAGACT 1200 CATCTGTGAA CAGACAGACA AGATTCCTGC CCTCCTAGGG CTTTTATTTC AATGGAAATA 1260 AAATACACAA ACAAGATTAT TTCTGATGGT TATAGTGCTC TGAAGGAAAT AAGAAGAGAA 1320 GTGAAAAGGT TTGGCTCTGA GGGTGGGCTA CTTTTGACAG CGGGTTCAGG GAAGATGCCT 1380 CTGAGTTGGC GATTGGGAAC TGAAGTCTGA AAGATGGGAG CTGAGGAAAG AGGGAACAGA 1440 AAATGCAACA GCCTTGAAGT GAGAACACCT GGAGCTTATT AGCAACAGAA AACCTGGAAC 1500 ACGATGGGGC AGAGAGTGAT GGGAGAGGAA GGCAGAGGTC AGCTTAGGAG TAGCTTTGTA 1560 ATGGTGTGAT TAAGTGTAAA 1580
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